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New types of metacaspases in phytoplankton reveal diverse origins of cell death proteases

机译:浮游植物中的新型代理酶揭示了细胞死亡蛋白酶的各种起源

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Metacaspases are evolutionarily distant homologs of caspases that are found outside the metazoan and are known to have key roles in programmed cell death (PCD). Two types of metacaspases (types I and II) have been defined in plants based on their domain structures; these have similarities to metazoan ‘initiator’ and ‘executioner’ caspases. However, we know little about metacaspases in unicellular organisms and even less about their roles in cell death. We identified a novel group of metacaspases in sequenced phytoplanktonic protists that show domain architectures distinct from either type I or II enzymes; we designate them as type III. Type III metacaspases exhibit a rearrangement of domain structures between N- and C-terminus. In addition, we found a group of metacaspase-like proteases in phytoplankton that show sequence homology with other metacaspases, but defy classification in conventional schemes. These metacaspase-like proteases exist in bacteria alongside a variant of type I metacaspases and we propose these bacterial metacaspases are the origins of eukaryotic metacaspases. Type II and III metacaspases were not detected in bacteria and they might be variants of bacterial type I metacaspases that evolved in plants and phytoplanktonic protists, respectively, during the establishment of plastids through the primary and secondary endosymbiotic events. A complete absence of metacaspases in protists that lost plastids, such as o?mycetes and ciliates indicates the gene loss during the plastid-to-nucleus gene transfer. Taken together, our findings suggest endosymbiotic gene transfer (EGT) is a key mechanism resulting in the evolutionary diversity of cell death proteases.
机译:Metacaspase asecassaspase是进化的遥远同源物的外壳,这些酶在美唑烷外发现,并且已知在编程的细胞死亡(PCD)中具有关键作用。基于其域结构,在植物中定义了两种类型的代表酶(类型I和II);这些与Metazoan'Initiator'和'刽子手'Caspases的相似之处。然而,我们对单细胞生物中的代表酶很少了解,甚至少于细胞死亡的角色。我们鉴定了一种新型的浮游植物基团组,其展示了与I型或II型酶不同的域架构;我们将它们指定为III型。 III型Metacaspase ass在N-和C-末端之间表现出域结构的重新排列。此外,我们在浮游植物中发现了一组Metacaspase样蛋白酶,其显示与其他金碱基酶的序列同源物,但在传统方案中缺乏分类。与I型代理酶的变体的细菌存在这些蛋白质样蛋白酶,我们提出这些细菌代表酶是真核代表酶的起源。在细菌中未检测到II型和III型选酶,它们可能是在通过初级和次生患者事件的体积建立体积期间分别在植物和植物和浮游植物中的细菌型代理酶的变体。在丢失塑性体的原实体中完全没有代理酶,例如O?霉菌和纤毛剂表明在塑体与细胞核基因转移过程中的基因损失。我们的研究结果表明,内酯基因转移(EGT)是一种关键机制,导致细胞死亡蛋白酶进化多样性。

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